A possible role for WRKY25 during defense signaling was further investigated by analyzing its expression in Arabidopsis after inoculation with PsmES4326.
We also characterized the relevance of AF-6 to PD by analyzing its expression in the brain of rats and patients.
We first determined whether TRAF1 is involved in liver I/R injury by analyzing its expression in ischemic lobes from mice subjected to warm liver I/R and from mice subjected to a sham procedure.
Finally, we investigated to which extent the "core UP" gene expression program from mature DC was specific to the activation of these cells as compared with shared responses with other immune cell types, by analyzing its expression in B cells, NK cells, and CD8+ T cells isolated from the same MCMV-infected or control animals.
However, the main goal of the current study was to evaluate PKC-β as a target of B lymphocyte malignancies by analyzing its expression across subtypes and correlation between expression and survival, and our results have clearly indicated that PKC-β could be an important target for B cell lymphoma chemotherapy.
To investigate whether Dot1L expression is also regulated by T3 during natural metamorphosis, we analyzed its expression by qRT-PCR in the intestine and tail at different stages from premetamorphic (stage 54), metamorphic climax (stages 58-64), thethendnd of metamorphosis (stage 66).
By homology searching, we identified the zebrafish sbds ortholog and then analyzed its expression by reverse transcriptase-polymerase chain reaction and in situ hybridization.
To explore the potential role of EphA5 in prostate carcinogenesis, we first analyzed its expression by real-time PCR in a panel of human nonmalignant (RWPE-1) and prostate cancer (LNCaP, LNCaP-LN3, PC-3, PC-3M-LN4, CWR22rv-1, and DU145) cell lines.
As a first step, we analyzed its expression pattern by Northern blot on a panel of RNA samples originating from tissues and cell lines.
*Not Determined In order to investigate Cav-1 expression in different stages of hepatocellular carcinogenesis, we analyzed its expression profile by immunoperoxidase staining of normal liver (n = 20), cirrhosis (n = 29), and HCC (n = 95) tissue samples.
To better understand the putative implication of FGFRL1 during embryonic development in chordates, we chose to analyze its expression pattern by whole mount in situ hybridization in two species: amphioxus, a cephalochordate placed at the base of the chordate clade; and mouse, a vertebrate for which only late embryonic expression has been described [ 22].
